Canonical Allele Identifier: CA009130

Gene: RET

Linked Data

• ClinVar Variation Id: 13922
• ClinVar RCV Id: RCV000014947
• dbSNP Id: rs76534745
• MyVariant Identifiers: chr10:g.43619231A>G (hg19) ; chr10:g.43123783A>G (hg38)
• PubMed: PMID:8114938

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43123783A>G , CM000672.2:g.43123783A>G	GRCh38
NC_000010.10:g.43619231A>G , CM000672.1:g.43619231A>G	GRCh37
NC_000010.9:g.42939237A>G	NCBI36
NG_007489.1:g.51715A>G , LRG_518:g.51715A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.2518A>G	ENSP00000480088.2:p.Arg840Gly
ENST00000683007.1:n.2488A>G
ENST00000340058.6:c.2914A>G	ENSP00000344798.4:p.Arg972Gly
ENST00000355710.8:c.2914A>G MANE Select	ENSP00000347942.3:p.Arg972Gly
ENST00000671844.1:c.*1508A>G	ENSP00000500541.1:n.*1508A>G
ENST00000672389.1:c.*1508A>G	ENSP00000500252.1:n.*1508A>G
ENST00000340058.5:c.2914A>G	ENSP00000344798.4:p.Arg972Gly
ENST00000355710.7:c.2914A>G	ENSP00000347942.3:p.Arg972Gly
ENST00000615310.4:c.*263A>G	ENSP00000480088.1:n.*263A>G
NM_020630.4:c.2914A>G , LRG_518t2:c.2914A>G	NP_065681.1:p.Arg972Gly
NM_020975.4:c.2914A>G , LRG_518t1:c.2914A>G	NP_066124.1:p.Arg972Gly
XM_011540027.1:c.2914A>G	XP_011538329.1:p.Arg972Gly
NM_001355216.1:c.2152A>G	NP_001342145.1:p.Arg718Gly
NM_020630.5:c.2914A>G	NP_065681.1:p.Arg972Gly
NM_020975.5:c.2914A>G	NP_066124.1:p.Arg972Gly
NM_020975.6:c.2914A>G MANE Select	NP_066124.1:p.Arg972Gly
NM_020630.6:c.2914A>G	NP_065681.1:p.Arg972Gly